Skip to main content
Log in

Function of plastoquinones B and C as electron acceptors in Photosystem II and fatty acid analysis of plastoquinone B

  • Published:
Photosynthesis Research Aims and scope Submit manuscript

Abstract

We have found that in petroleum-ether extracted tobacco thylakoids, plastoquinone A (PQ-A) and plastoquinone C (PQ-C) had similar efficiency in restoration of oxygen-evolving activity, while plastoquinone B (PQ-B), which is a fatty acid ester of PQ-C, was about 50% less effective. This indicates that apart from PQ-A, PQ-C and to a smaller extent PQ-B may function as electron acceptors of Photosystem II (PS II). The DCMU inhibition curves for PQ-C and PQ-B were biphasic and an initial slow decline was followed by a sharp decrease in oxygen evolution yield with a 50% inhibition (I50) at 0.25 μM DCMU. In the case of PQ-A (I50 = 0.20 μM DCMU), the activity decreased gradually without the sharp transition. The corresponding inhibition curve for unextracted thylakoids, where all the native prenylquinones are present, shows an intermediate shape between PQ-A and PQ-C but with a higher I50, equal to 0.32 μM, suggesting that the contribution of PQ-C as an electron acceptor of Photosystem II might be significant in thylakoid membranes with natural prenyllipid composition. α-Tocopherol quinone showed no activity in the restoration of oxygen evolution in extracted thylakoids, indicating that it cannot accept electrons from PS II. The fatty acid composition of PQ-B isolated from maple leaves showed a high degree of saturated fatty acids like myristic and palmitic acid, and its unique composition indicates that it is a natural component of the thylakoid membrane.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Barr R and Crane FL (1971) Quinones in algae and higher plants. Methods Enzymol 23A: 372–408

    Google Scholar 

  • Barr R and Crane FL (1977) Evidence for α-tocopherol function in the electron transport chain of chloroplasts. Plant Physiol 59: 433–436

    Google Scholar 

  • Barr R, Henninger MD and Crane FL (1967) Comparative studies on plastoquinone II. Analysis for plastoquinones A, B, C and D. Plant Physiol: 42, 1246–1254

    Google Scholar 

  • Cox RP and Bendall DS (1974) The functions of plastoquinone and β-carotene in Photosystem II of chloroplasts. Biochim Biophys Acta 347: 49–59

    Google Scholar 

  • Das BC, Lounasmaa M, Tendille C and Lederer E (1967) The structure of the plastoquinones B and C. Biochem Biophys Res Commun 26: 211–215

    Google Scholar 

  • Griffiths WT, Wallwork JC and Pennock FJ (1966) Presence of a series of plastoquinones in plants. Nature 211: 1037–1039

    Google Scholar 

  • Gruszecki WI, Strzałka K, Radunz A, Kruk J and Schmid GH (1995) Blue light-enhanced photosynthetic oxygen evolution from liposome-bound photosystem II particles; possible role of the xantophyll cycle in the regulation of cyclic electron flow around Photosystem II? Z Naturforsch 50c: 61–68

    Google Scholar 

  • He P, Radunz A, Bader KP and Schmid GH (1996) Quantitative changes of the lipid and fatty acid composition of leaves of Aleurites montana as a consequence of growth under 700 ppm CO2 in the atmosphere. Z Naturforsch 51c: 833–840

    Google Scholar 

  • Henninger MD and Crane FL (1966) I. A combined requirement for plastoquinones A and C for photoreduction of 2,6-dichloroindophenol. J Biol Chem 241: 5190–5196

    Google Scholar 

  • Henninger MD and Crane FL (1967) III. The role of plastoquinone C. J Biol Chem 242: 1155–1159

    Google Scholar 

  • Henninger MD, Barr R and Crane FL (1966) Plastoquinone B. Plant Physiol 41: 696–700

    Google Scholar 

  • Hurt E and Hauska G (1982) Involvement of plastoquinone bound within the isolated cytochrome b6-f complex from chloroplasts in oxidant-induced reduction of cytochrome b6. Biochim Biophys Acta 682: 466–473

    Google Scholar 

  • Karukstis K, Berliner MA, Jewell CJ and Kuwata KT (1990) Competition of anthraquinones for the QB binding domain. In: Baltscheffsky M (ed) Curr Res Photosynth, Vol 1, pp 579–582. KluwerAcademic Publishers

  • Koike H, Yamashita M, Kashino Y and Satoh K (1995) Mechanism of electron flow through the QB site in Photosystem II. Analysis of reaction mechanism at the QB and PQ site in Photosystem II core complexes. In: Mathis P (ed) Photosynthesis: from Light to Biosphere, Vol. 1, pp 623–626. Kluwer Academic Publishers

    Google Scholar 

  • Kruk J (1988) Charge-transfer complexes of plastoquinone and α-tocopherol quinone in vitro. Biophys Chem 30: 143–149

    Google Scholar 

  • Kruk J and Strzałka K (1995) The function of α-tocopherol quinone in biological systems. J Plant Physiol 145: 405–409

    Google Scholar 

  • Kruk J and Strzałka K (1998) Identification of plastoquinone-C in spinach and maple leaves by reverse-phase high-performance liquid chromatography. Phytochemistry, (in press)

  • Kruk J, Strzałka K and Leblanc RM (1992) Monolayer study of plastoquinones, α-tocopherolquinone, their hydroquinone forms and their interaction with monogalactosyldiacylglycerol. Biochim Biophys Acta 1112: 19–26

    Google Scholar 

  • Kruk J, Burda K, Radunz A, Strzałka K and Schmid GH (1997) Antagonistic effects of α-tocopherol and α-tocoquinone in the regulation of cyclic electron transport around Photosystem II. Z Naturforsch 52c: 766–744

    Google Scholar 

  • Lichtenthaler HK (1977) Regulation of prenylquinone synthesis in higher plants. In: Tevini M and Lichtenthaler HK (eds) Lipids and Lipid Polymers in Higher Plants, pp 231–258. Springer Verlag, Berlin, Heidelberg, New York

    Google Scholar 

  • Lichtenthaler HK and Calvin M (1964) Quinone and pigment composition of chloroplasts and quantosome aggregates from Spinacia oleracea. Biochim Biophys Acta 79: 30–40

    Google Scholar 

  • Magree L, Henninger MD and Crane FL (1966) II. Effect of hydrocarbon solvent extraction on chloroplast membrane structure. J Biol Chem 241: 5197–5200

    Google Scholar 

  • Michalski WP and Kaniuga Z (1981) Photosynthetic apparatus of chilling-sensitive plants. IX. The involvement of α-tocopherol in the electron transport chain and the anti-oxidizing system in chloroplasts of tomato leaves. Biochim Biophys Acta 635: 25–37

    Google Scholar 

  • Okayama S (1983) Studies on quinones in green leaves. In: Inoue Y, Murata N, Crofts AR, Renger G, Govindjee and Satoh K (eds) The Oxygen Evolving System of Photosynthesis, pp 393–400. Academic Press, Tokyo

    Google Scholar 

  • Okayama S (1984) Reverse-phase high-performance liquid chromatography of prenylquinones in green leaves using an electrochemical detector. Plant Cell Physiol 25: 1445–1449

    Google Scholar 

  • Okayama S and Butler WL (1972) Extraction and reconstitution of Photosystem II. Plant Physiol 49: 769–774

    Google Scholar 

  • Rich PR and Moss DA (1987) The reactions of quinones in higher plant photosynthesis. In: Barber J (ed) The Light Reactions, pp 421–445. Elsevier, Amsterdam

    Google Scholar 

  • Robinson HH and Yocum CF (1980) Cyclic photophosphorylation reactions catalyzed by ferredoxin, methyl viologen and anthraquinone sulfonate. Biochim Biophys Acta 590: 97–106

    Google Scholar 

  • Sadewasser DA and Dilley RA (1978) A dual requirement for plastoquinone in chloroplast electron transport. Biochim Biophys Acta 501: 208–216

    Google Scholar 

  • Satoh K, Kitatani Y, Ichimura T and Katoh S (1990) Interactions between various benzoquinones and the QB site of oxygen evolving photosystem II preparations from the thermophilic cyanobacterium Synechococcus elongatus. In: Baltscheffsky M (ed) Current Research in Photosynthesis, Vol 1, pp 583–586. Kluwer Academic Publishers, Dordrecht, The Netherlands

    Google Scholar 

  • Schmid GH and Thibault P (1979) Evidence for a rapid oxygen uptake in tobacco chloroplasts. Z Naturforsch 34c: 414–418

    Google Scholar 

  • Sun E, Barr R and Crane FL (1968) Comparative studies on plastoquinones. IV. Plastoquinones in algae. Plant Physiol 43: 1935–1940

    Google Scholar 

  • Tabata K, Itoh S, Yamamoto Y, Okayama S and Nishimura M (1985) Two plastoquinone A molecules are required for Photosystem II activity; analysis in hexane-extracted Photosystem II particles. Plant Cell Physiol 26: 855–863

    Google Scholar 

  • Trebst A (1986) The topology of the plastoquinone and herbicide binding peptides of Photosystem II in the thylakoid membrane. Z Naturforsch 41c: 240–245

    Google Scholar 

  • Wi¸eckowski S and Bojko M (1997) The NADPH-dependent electron flow in chloroplasts of the higher plants. Photosynthetica 34: 481–496

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kruk, J., Burda, K., Schmid, G.H. et al. Function of plastoquinones B and C as electron acceptors in Photosystem II and fatty acid analysis of plastoquinone B. Photosynthesis Research 58, 203–209 (1998). https://doi.org/10.1023/A:1006139227593

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1006139227593

Navigation